42 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pfkmem1(IMPC)Mbp/Pfkm+ C57BL/6N-Pfkmem1(IMPC)Mbp/MbpMmucd	abnormal liver morphology	J:211773
	abnormal seminal vesicle morphology	J:211773
	abnormal skin morphology	J:211773
	abnormal testis morphology	J:211773
	abnormal vitreous body morphology	J:211773
	decreased body length	J:211773
	decreased total body fat amount	J:211773
	enlarged testis	J:211773
	increased lean body mass	J:211773
	small liver	J:211773
	small seminal vesicle	J:211773
PfkmGT(OST56064)Lex/PfkmGT(OST56064)Lex involves: 129S5/SvEvBrd * C57BL/6	abnormal glucose homeostasis	J:125530
	decreased circulating insulin level	J:125530
	decreased insulin secretion	J:125530
	impaired glucose tolerance	J:125530
	increased circulating glucose level	J:125530
Pfkmtm1Fbos/Pfkmtm1Fbos involves: 129S6/SvEvTac * C57BL/6J	abnormal angiogenesis	J:152153
	abnormal glucose homeostasis	J:152153
	abnormal muscle physiology	J:152153
	abnormal skeletal muscle fiber morphology	J:152153
	cardiac hypertrophy	J:152153
	centrally nucleated skeletal muscle fibers	J:152153
	decreased circulating lactate level	J:152153
	decreased hematocrit	J:152153
	enhanced skeletal muscle regeneration	J:152153
	enlarged heart	J:152153
	enlarged spleen	J:152153
	heart left ventricle hypertrophy	J:152153
	hypoxia	J:152153
	impaired exercise endurance	J:152153
	increased cardiac muscle glycogen level	J:152153
	increased circulating bilirubin level	J:152153
	increased erythrocyte osmotic fragility	J:152153
	increased heart weight	J:152153
	increased hematopoietic stem cell number	J:152153
	increased lactate dehydrogenase level	J:152153
	increased skeletal muscle glycogen level	J:152153
	increased spleen weight	J:152153
	lethality at weaning, incomplete penetrance	J:152153
	premature death	J:152153
	reticulocytosis	J:152153
	skeletal muscle fiber degeneration	J:152153
	skeletal muscle fiber necrosis	J:152153